酚醛胺(T-31)环氧树脂固化剂之浅谈

介绍了酚醛胺(T-31)系列环氧固化剂及原料的现状和特点,并对酚醛胺(T-31)系列环氧固化剂进行了分代,阐述了第三代酚醛胺(T-31)系列环氧固化剂的系列化、专用化、高档化。预测和展望了2005年的需求和方向。     

聚硅氧烷改性环氧树脂的研究进展

综述了制备聚有机硅氧烷改性环氧树脂的4种途径：含羟基或烷氧基的聚硅氧烷与环氧树脂的反应、含氨基的聚硅氧烷与环氧树脂的反应、含硅氢基的聚硅氧烷与环氧树脂的反应、含杂原子的聚硅氧烷与环氧树脂的反应,并讨论了聚有机硅氧烷改性环氧树脂对环氧树脂的相结构、机械性能和热稳定性的影响.     

环氧稀释剂十二烷基缩水甘油醚的合成

对稀释剂十二烷基缩水甘油醚的合成及影响产品质量的因素进行了研究,并以十二、十四混醇为原料进行了对比试验。     

纳米SiO_2粒子在环氧树脂中的分散工艺研究

研究了纳米SiO2在环氧树脂中的均匀分散工艺,探讨了超声波振荡和超声波分散时间对纳米SiO2/EP复合材料力学性能的影响,确定了最佳分散工艺。SEM表明,采用高剪切与超声波复合分散工艺比高剪切工艺的分散效果好;测试了复合材料的力学性能,进一步证明纳米SiO2具有增韧增强作用。     

碳钢贮热水箱的模拟腐蚀试验及涂层耐蚀性能研究

碳钢贮热水箱长期在30～80°C温变的热水环境中工作,易受到热水及水中杂质的腐蚀。研究了不同温度下Q235钢在自来水及含100μg/mLNaCl的自来水中的腐蚀速率。对裸钢及其涂覆相同厚度的不同涂层──酚醛环氧(自制)、钛纳米聚合物和改性聚乙烯后在70°C自来水中的极化曲线进行了比较。采用动电位扫描极化曲线测量和电化学交流阻抗谱法(EIS)分别对涂覆不同涂层的Q235钢进行了耐蚀性能研究。结果表明,3种防腐涂层均具有较佳的抗热水性,耐蚀能力较强,适宜对Q235钢贮热水箱进行防护。     

Influences of zinc oxide and an organic additive on the electrochemical behavior of pure aluminum in an alkaline solution

The corrosion behavior of pure aluminum in inhibited and uninhibited 4 MKOH was investigated by means of hydrogen collection, polarization curve measurement and electrochemical impedance spectroscopy (EIS). The results showed that the corrosion of pure aluminum was greatly inhibited by the addition of ZnO and dimethyl amine epoxy propane (designated as DE). EIS and EDAX analyses revealed that ZnO produces its effect by depositing on the aluminum surface, which increases the overpotential of hydrogen evolution. It was also found that the addition of DE could greatly improve the deposition of zinc layers.     

环氧-聚氨酯互穿网络防腐蚀涂料

研制的环氧-聚氨酯互穿网络(IPN)防腐蚀涂料具有优异的防腐蚀性能和附着力。介绍了该涂料的制法。列举了IPN涂层的性能指标。讨论了影响涂层性能的各种因素。     

集成电路密封用高纯邻甲酚醛环氧树脂的制备

ECN树脂中的可水解氯含量是决定树脂质量的—个重要指标。本文研究了反应温度、ECH/OCN配比、反应时间和碱用量等因素的影响,取得了规律性的认识,并获得最佳配方,制备出高纯度的ECN树脂系列产品。     

Crystallization,morphology, structure and thermal behaviour of nylon-6/rubber blends

An experimental study was carried out in order to investigate the morphological, kinetic, structural and thermodynamic properties of nylon-6/rubber (namely ethylene-propylene copolymer (EPM) and ethylene-propylene copolymer functionalized by inserting along its backbone succinic anhydride groups (EPM-g-SA)) blends. The morphology and the overall kinetics of crystallization of the blends strongly depend on the type of copolymer added to nylon and on the blend composition. The EPM-g-SA acts as a nucleating agent for the Ny spherulites and at the same time causes a drastic depression of the overall kinetic rate constant. This decrease is related to the increase of the melt viscosity observed in Ny/EPM-g-SA blends. The crystalline lamella thickness of the Ny phase in the blends is lower than that of pure Ny crystallized at the same T_c suggesting that the presence in the melt of an elastomeric phase disturbs the growth of the Ny crystals. The rubber does not influence the thermal behaviour of the nylon. The results found lead to the conclusion that in the melt nylon-6 is incompatible with both EPM and EPM-g-SA copolymers.